Open Access
Open access
Environmental DNA, volume 7, issue 1

Fish eDNA Composition Along a Gradient of Freshwater eDNA in an Estuarine Bay

Shota Homma 1
Shinya Hosokawa 1, 2
T. Komuro 3
1
 
Big Data Technology Group Port and Airport Research Institute Yokosuka Kanagawa Japan
2
 
Marine Environmental Information Group Port and Airport Research Institute Yokosuka Kanagawa Japan
3
 
College of Economics Kanto Gakuin University Yokohama Kanagawa Japan
Publication typeJournal Article
Publication date2025-01-29
scimago Q1
SJR2.043
CiteScore11.0
Impact factor
ISSN26374943
Abstract
ABSTRACT

Metabarcoding of environmental DNA (eDNA) is becoming practically applied to fish monitoring and conservation surveys in estuaries. However, estuarine bays may be an unsuitable zone to use eDNA metabarcoding because they are affected by eDNA originating from upstream rivers. In this study, the transition of eDNA composition from river to bay was examined to investigate the influence of freshwater sources on the eDNA composition of the downstream bay. Samples were collected in a bay spanning around 1 km and an upstream river under high and low tide within 1 day in November and in January. The samples were analyzed by using eDNA metabarcoding for fish species and species‐specific quantitative analysis for the freshwater fish Cyprinus carpio. Our findings reveal that the eDNA of freshwater fishes was drastically diluted in the model estuarine bay. As a result, the relative‐read‐based composition clearly changed from riverine to marine environments, and the freshwater inflow had little effect on the relative‐read‐based composition at those sites. However, eDNA from freshwater fishes was widely detected in the bay by species‐specific and metabarcoding analysis, suggesting that fresh water may have a more significant impact when focusing on presence/absence‐based composition. Our study also found that the transition zone for the concentration of freshwater eDNA fluctuated spatiotemporally with tides, indicating that the degree of influence from the river varies with tide. Therefore, prior measurement of the distribution of freshwater fish eDNA at low tide would help to conservatively determine better sampling sites and design more reliable sampling in estuaries.

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